scholarly journals Mesenchymal Stem or Stromal Cells from Amnion and Umbilical Cord Tissue and Their Potential for Clinical Applications

Cells ◽  
2012 ◽  
Vol 1 (4) ◽  
pp. 1061-1088 ◽  
Author(s):  
Andrea Lindenmair ◽  
Tim Hatlapatka ◽  
Gregor Kollwig ◽  
Simone Hennerbichler ◽  
Christian Gabriel ◽  
...  
2015 ◽  
Vol 9 (Suppl 9) ◽  
pp. P65
Author(s):  
Irene Oliver-Vila ◽  
Maria I Coca ◽  
Marta Grau-Vorster ◽  
Noelia Pujals-Fonts ◽  
Marta Caminal ◽  
...  

2020 ◽  
Vol 9 (10) ◽  
pp. 1137-1146 ◽  
Author(s):  
Jessica M. Sun ◽  
Geraldine Dawson ◽  
Lauren Franz ◽  
Jill Howard ◽  
Colleen McLaughlin ◽  
...  

2011 ◽  
Vol 2011 ◽  
pp. 1-9 ◽  
Author(s):  
Eder Zucconi ◽  
Natassia Moreira Vieira ◽  
Carlos Roberto Bueno ◽  
Mariane Secco ◽  
Tatiana Jazedje ◽  
...  

Umbilical cord mesenchymal stromal cells (MSC) have been widely investigated for cell-based therapy studies as an alternative source to bone marrow transplantation. Umbilical cord tissue is a rich source of MSCs with potential to derivate at least muscle, cartilage, fat, and bone cellsin vitro. The possibility to replace the defective muscle cells using cell therapy is a promising approach for the treatment of progressive muscular dystrophies (PMDs), independently of the specific gene mutation. Therefore, preclinical studies in different models of muscular dystrophies are of utmost importance. The main objective of the present study is to evaluate if umbilical cord MSCs have the potential to reach and differentiate into muscle cellsin vivoin two animal models of PMDs. In order to address this question we injected (1) human umbilical cord tissue (hUCT) MSCs into the caudal vein ofSJLmice; (2) hUCT and canine umbilical cord vein (cUCV) MSCs intra-arterially in GRMD dogs. Our results here reported support the safety of the procedure and indicate that the injected cells could engraft in the host muscle in both animal models but could not differentiate into muscle cells. These observations may provide important information aiming future therapy for muscular dystrophies.


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